{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA071583"
        ],
        "brand_name": [
          "DIAZEPAM"
        ],
        "generic_name": [
          "DIAZEPAM"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-3213"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAMUSCULAR",
          "INTRAVENOUS"
        ],
        "substance_name": [
          "DIAZEPAM"
        ],
        "rxcui": [
          "309845"
        ],
        "spl_id": [
          "2d6df2eb-55ce-4d78-b268-99cbb512a687"
        ],
        "spl_set_id": [
          "7e7dd743-a87b-4ab3-b6ae-f116cd0c8b0f"
        ],
        "package_ndc": [
          "0409-3213-11",
          "0409-3213-12"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "N0000175694",
          "M0002356"
        ],
        "pharm_class_epc": [
          "Benzodiazepine [EPC]"
        ],
        "pharm_class_cs": [
          "Benzodiazepines [CS]"
        ],
        "unii": [
          "Q3JTX2Q7TU"
        ]
      },
      "product_type": "Drugs",
      "event_id": "66104",
      "recalling_firm": "Hospira Inc.",
      "address_1": "275 N Field Dr",
      "address_2": "",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-927-2013",
      "product_description": "Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only, Hospira, Inc., Lake Forest, IL 60045, USA,  NDC 0409-3213-12",
      "product_quantity": "72,300 vials",
      "reason_for_recall": "Lack of assurance of sterility: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials.",
      "recall_initiation_date": "20130816",
      "center_classification_date": "20130828",
      "termination_date": "20141028",
      "report_date": "20130904",
      "code_info": "Lot: 23-505-EV, Exp. 11/14",
      "more_code_info": ""
    }
  ]
}